Analysis of transforming growth factor beta 1 (TGF-β1) gene polymorphisms in Turkish patients with scleroderma


Büyük U., Ates Ö., DALYAN L., Müsellim B., Öngen G., TOPAL SARIKAYA A.

Cell Biochemistry and Function, vol.28, no.4, pp.274-277, 2010 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 28 Issue: 4
  • Publication Date: 2010
  • Doi Number: 10.1002/cbf.1649
  • Journal Name: Cell Biochemistry and Function
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.274-277
  • Keywords: Fibrosis, Lung involvement, Polymorphism, Scleroderma, TGF-β1
  • İstanbul Yeni Yüzyıl University Affiliated: No

Abstract

Systemic sclerosis (SSc) is an autoimmune disease characterized by inflammation and fibrosis of the skin and visceral organs. Fibrosis associated with SSc is characterized by an increased synthesis of a wide range of extracellular matrix (ECM). TGF-β is a pluripotent cytokine in a wide range of cell types. In particular it has been found to be a potent inducer of ECM protein synthesis and fibroblast migration. The TGF-β1 geneis highly polymorphic and two signal sequence polymorphisms at codon10 and codon 25 are linked to disease outcomes. In this study, we analysed two polymorphic sites of the TGF-β1 gene, codon 10 and codon 25, in 43 Turkish SSc female patients with interstitial lung involvement and in 75 healty individuals by ARMS-PCR. In our study no significant difference was found in codon 10, codon 25 genotype frequencies between patient with SSc and the control group (p = 0.676, 0.375, respectively). Our findings suggest that codon 10 and 25 polymorphism cannot be related with SSc for Turkish population. Copyright © 2010 John Wiley & Sons, Ltd.